Castor EDC

1. Patients use a connected glucometer to measure glucose levels at home.

2. Data is automatically transmitted to Castor EDC via API.

3. Real-time alerts are triggered for out-of-range readings.

4. Investigators review patient data and provide remote support.

5. Data is analyzed for efficacy and safety endpoints.

1. Patients are recruited and consented remotely using eConsent.

2. Patients report symptoms and quality of life via ePRO.

3. Clinical data is collected at local clinics and entered into Castor EDC.

4. Centralized monitoring and data review are performed remotely.

5. Data is analyzed to assess treatment outcomes.

1. Data from sensors, wearables, and patient diaries is integrated into Castor EDC.

2. Data quality checks and validation rules are implemented.

3. Compliance reports are generated automatically.

4. Data is analyzed to optimize device performance.

5. Submission-ready datasets are created for regulatory filings.

1. Researchers design and build their study database using Castor EDC's self-service platform.

2. Data is collected from patients and entered directly into the system.

3. Simple reports and data visualizations are generated.

4. Data is exported for statistical analysis.

5. Results are published in peer-reviewed journals.

1. Implement Castor's functional oversight framework.

2. Document all processes and procedures.

3. Conduct regular risk assessments.

4. Monitor data quality and integrity.

5. Ensure proper training for all study personnel.